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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1028537생성일: 2026년 10월 24일

Sodium bis(trimethylsilyl)amide → (4S,5S)-5-[3,5-bis(trifluoromethyl)phenyl]-3-{[5'-isopropyl-2'-methoxy-4-(trifluoromethyl)biphenyl-2-yl]methyl}-4-methyl-1,3-oxazolidin-2-one

https://huagongshe.com/ko/reaction/1028537

반응식

참여 물질

역할이름HCID투입량
반응물Sodium bis(trimethylsilyl)amideHCID 2724254—
반응물2-(Bromomethyl)-5'-isopropyl-2'-methoxy-4-(trifluoromethyl)biphenylHCID 53363643—
반응물(4S,5S)-5-[3,5-bis(trifluoromethyl)phenyl]-4-methyl-1,3-oxazolidin-2-oneHCID 86603412—
용매TetrahydrofuranHCID 8028—
용매DimethylacetamideHCID 31374—
생성물(4S,5S)-5-[3,5-bis(trifluoromethyl)phenyl]-3-{[5'-isopropyl-2'-methoxy-4-(trifluoromethyl)biphenyl-2-yl]methyl}-4-methyl-1,3-oxazolidin-2-oneHCID 53363913—

반응 단계

((4S,5S)-5-[3,5-bis(trifluoromethyl)phenyl]-4-methyl-1,3-oxazolidin-2-one) (46.2 mg, 0.148 mmol) was placed in a dry flask and DMA (3 mL) was added. NaHMDS (296 μL of a 1M solution in THF, 0.296 mmol) was added and the reaction was stirred for 5 min. At this time, 2′-(bromomethyl)-5-isopropyl-4′-(trifluoromethyl)biphenyl-2-yl methyl ether (80.0 mg, 0.207 mmol) was added by cannula in DMA (2 mL). After 30 min, the reaction was quenched with saturated NH4Cl (2 mL). The mixture was diluted with EtOAc (40 mL). The organic layer was washed with water (15 mL), and brine (15 mL), dried over Na2SO4, filtered, and concentrated. Purification of the residue by flash chromatography with 25% EtOAc/hexanes afforded (4S,5S)-5-[3,5-bis(trifluoromethyl)phenyl]-3-{[5′-isopropyl-2′-methoxy-4-(trifluoromethyl)biphenyl-2-yl]methyl}-4-methyl-1,3-oxazolidin-2-one. Rf=0.27 (25% EtOAc/hexanes). LCMS=620.2 (M+1)+. 1H NMR (CDCl3, 500 MHz; atropisomers present) δ 6.90-7.88 (m, 9H), 4.04-5.05 (m, 3H), 3.25-3.74 (m, 4H), 2.88 (m, 1H), 1.19-1.24 (m, 6H), 0.99-1.07 (m, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08735435B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-b81eecf43c794f8595c0db2b5fdd982f
출처 메모uspto-grants-2014_05